ClinVar Miner

Submissions for variant NM_000368.4(TSC1):c.1109C>T (p.Ser370Leu) (rs796053457)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000189845 SCV000243498 uncertain significance not provided 2013-11-22 criteria provided, single submitter clinical testing p.Ser370Leu (TCA>TTA): c.1109 C>T in exon 11 of the TSC1 gene (NM_000368.4). The Ser370Leu missense change in the TSC1 gene has not been published as a mutation, nor has it been reported as a benign polymorphism to our knowledge. It was not observed in approximately 6,500 individuals of European and African American ancestry in the NHLBI Exome Sequencing Project, indicating it is not a common benign variant in these populations. This variant is a non-conservative amino acid substitution of a polar Serine residue with a non-polar Leucine residue. However, it alters a position that is not highly conserved across species and Leucine is observed at this position in distantly related species. In silico analysis is inconsistent with regard to the effect this variant may have on the protein structure/function. Additionally, the vast majority of TSC1 mutations result in protein truncation, while missense mutations have been reported only rarely (Northrup et al., 2011; Au et al., 2007). Therefore, based on the currently available information, it is unclear whether Ser370Leu is a disease-causing mutation or a rare benign variant. The variant is found in INFANT-EPI panel(s).

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